Development of Biogenic Silver Nanoparticle Using Rosa Chinensis Flower Extract and Its Antibacterial Property.

In the present study, biosynthesis of silver nanoparticles was carried out using Rosa chinensis flower extract as reducing agent. The characterization of silver nanoparticles was done by UV-VIS spectrum. The morphology and size of silver nanoparticles were determined by transmission electron microscope (TEM) image. The crystallization of silver nanoparticles was confirmed by X-ray diffraction (XRD) measurements. The Fourier transform infrared (FT-IR) analysis was used to confirm the possible involvement in the formation and stabilization of synthesized silver nanoparticles by the extract of Rosa chinensis flower. Antibacterial activity of silver nanoparticles was studied against Gram positive Staphycoccus aureus and Gram negative Escherichia coil.

Synthesis and Adsorption Property of SiO2@Co(OH)2 Core-Shell Nanoparticles.

Silica nanoparticles were directly coated with cobalt hydroxide by homogeneous precipitation of slowly decomposing urea in cobalt nitrate solution. The cobalt hydroxide was amorphous, and its morphology was nanoflower-like. The BET (Brunauer-Emmett-Teller) surface area of the core-shell composite was 221 m²/g. Moreover, the possible formation procedure is proposed: the electropositive cobalt ions were first adsorbed on the electronegative silica nanoparticles surface, which hydrolyzed to form cobalt hydroxide nanoparticles. Then, the cobalt hydroxide nanoparticles were aggregated to form nanoflakes. Finally, the nanoflakes self-assembled, forming cobalt hydroxide nanoflowers. Adsorption measurement showed that the core-shell composite exhibited excellent adsorption capability of Rhodamine B (RB).

A Sustainable Approach to Fabricating Ag Nanoparticles/PVA Hybrid Nanofiber and Its Catalytic Activity.

Ag nanoparticles were synthesized by using Ficus altissimaBlume leaf extract as a reducing agent at room temperature. The resulting Ag nanoparticles/PVA mixture was employed to create Ag nanoparticles/PVA (polyvinyl alcohol) hybrid nanofibers via an electrospinning technique. The obtained nanofibers were confirmed by means of UV-Vis spectroscopy, The X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and then tested to catalyze KBH4 reduction of methylene blue (MB). The catalytic results demonstrate that the MB can be reduced completely within 15 min. In addition, the Ag nanoparticles/PVA hybrid nanofibers show reusability for three cycles with no obvious losses in degradation ratio of the MB.

Smart gold nanoparticles enhance killing effect on cancer cells.

The present study explored the cellular uptake dynamics, the subcellular location and the internalization mechanisms of gold nanoparticles (GNPs) and glucose-capped GNPs (Glu-GNPs). The cancer radiotherapy-enhancing effects of GNPs were also evaluated. We synthesized the GNPs and Glu-GNPs by the seeding technique. The effects on cellular uptake and the radiosensitizing effect induced by GNPs and Glu-GNPs at lower doses were investigated using two human cancer cell lines (HeLa and MCF-7). The intracellular location of the nanoparticles was analyzed by transmission electron microscopy (TEM). Analysis of cellular apoptosis following GNP-based radiotherapy was performed by flow cytometry and TUNEL assay. Cancer cells took up more Glu-GNPs than naked GNPs and the uptake curve showed size- and cell-dependent uptake. GNPs were mainly located in the cytoplasm and endocytosis is the mechanism behind the internalization of GNPs and Glu-GNPs. Lower doses of GNPs and Glu-GNPs still enhanced the killing effect using X-ray irradiation, although the apoptotic rate was not altered. The results presented in this study provide evidence that Glu-GNPs may have a bright future in tumor-targeted diagnosis and treatment.

Water-soluble and biocompatible sono/photosensitizer nanoparticles for enhanced cancer therapy.

AIMS: Most sono/photosensitizers of cancer sonodynamic/photodynamic therapy (SDT/PDT), such as hypocrellin SL052, are water-insoluble, therefore restricting their clinical applications. In this article, we present a water-soluble nanocarrier to load the SDT/PDT sensitizer SL052 with improved pharmacokinetics and therapeutic efficacy. MATERIALS & METHODS: Nanoclusters of polyvinylpyrrolidones with SL052 formed water-soluble nanoparticles (SL052-NPs) while retaining the chemical structure of SL052. RESULTS: The experimental results show that SL052-NPs improve the drug's physicochemical properties and significantly enhance the efficacy of SL052 in terms of pharmacokinetics and cancer killing. Water-soluble SL052-NPs can be used to deliver the drug to deep cancer tissues. A potential benefit of SL052-NPs is that polyvinylpyrrolidones can help SL052 evade the reticuloendothelial system, thereby increasing circulation half-life and improving drug biodistribution. CONCLUSION: SL052-NPs greatly improved the physicochemical properties of SL052 without modifying its chemical structure, allowing for deep-site cancer drug delivery, imaging for diagnosis, and ultrasound or photocontrolled localized cancer therapy.

Fabrication and characterization of mesoporous Co3O4 core/mesoporous silica shell nanocomposites.

A mesoporous Co(3)O(4) core/mesoporous silica shell composite with a variable shell thickness of 10-35 nm was fabricated by depositing silica on Co(3)O(4) superlatticed particles. The Brunauer-Emmett-Teller (BET) surface area of the composite with a shell thickness of ca. 2.0 nm was 238.6 m(2)/g, which varied with the shell thickness, and the most frequent pore size of the shell was ca. 2.0 nm. After the shell was eroded with hydrofluoric acid, mesoporous Co(3)O(4) particles with a pore size of ca. 8.7 nm could be obtained, whose BET surface area was 86.4 m(2)/g. It is proposed that in the formation of the composite the electropositive cetyltrimethylammonium bromide (CTAB) micelles were first adsorbed on the electronegative Co(3)O(4) particle surface, which directed the formation of the mesoporous silica on the Co(3)O(4) particle surface. Electrochemical measurements showed that the core/shell composites exhibited a higher discharge capacity compared with that of the bare Co(3)O(4) particles.